A citation-based method for searching scientific literature

Amany I Gorgy, Naudia L Jonassaint, Susan E Stanley, Ayman Koteish, Amy E DeZern, Jolan E Walter, Sabrina C Sopha, James P Hamilton, Julie Hoover-Fong, Allen R Chen, Robert A Anders, Ihab R Kamel, Mary Armanios. Chest 2015
Times Cited: 47







List of co-cited articles
369 articles co-cited >1



Times Cited
  Times     Co-cited
Similarity


Lung transplantation in telomerase mutation carriers with pulmonary fibrosis.
Leann L Silhan, Pali D Shah, Daniel C Chambers, Laurie D Snyder, Gerdt C Riise, Christa L Wagner, Eva Hellström-Lindberg, Jonathan B Orens, Juliette F Mewton, Sonye K Danoff,[...]. Eur Respir J 2014
101
42

Exome sequencing identifies mutant TINF2 in a family with pulmonary fibrosis.
Jonathan K Alder, Susan E Stanley, Christa L Wagner, Makenzie Hamilton, Vidya Sagar Hanumanthu, Mary Armanios. Chest 2015
88
38

Telomerase mutations in families with idiopathic pulmonary fibrosis.
Mary Y Armanios, Julian J-L Chen, Joy D Cogan, Jonathan K Alder, Roxann G Ingersoll, Cheryl Markin, William E Lawson, Mingyi Xie, Irma Vulto, John A Phillips,[...]. N Engl J Med 2007
791
38

Syndrome complex of bone marrow failure and pulmonary fibrosis predicts germline defects in telomerase.
Erin M Parry, Jonathan K Alder, Xiaodong Qi, Julian J-L Chen, Mary Armanios. Blood 2011
98
36

Loss-of-function mutations in the RNA biogenesis factor NAF1 predispose to pulmonary fibrosis-emphysema.
Susan E Stanley, Dustin L Gable, Christa L Wagner, Thomas M Carlile, Vidya Sagar Hanumanthu, Joshua D Podlevsky, Sara E Khalil, Amy E DeZern, Maria F Rojas-Duran, Carolyn D Applegate,[...]. Sci Transl Med 2016
96
36

The gastrointestinal manifestations of telomere-mediated disease.
Naudia L Jonassaint, Nini Guo, Joseph A Califano, Elizabeth A Montgomery, Mary Armanios. Aging Cell 2013
55
34

A spectrum of severe familial liver disorders associate with telomerase mutations.
Rodrigo T Calado, Joshua A Regal, David E Kleiner, David S Schrump, Nathan R Peterson, Veronica Pons, Stephen J Chanock, Peter M Lansdorp, Neal S Young. PLoS One 2009
122
31

Exome sequencing links mutations in PARN and RTEL1 with familial pulmonary fibrosis and telomere shortening.
Bridget D Stuart, Jungmin Choi, Samir Zaidi, Chao Xing, Brody Holohan, Rui Chen, Mihwa Choi, Pooja Dharwadkar, Fernando Torres, Carlos E Girod,[...]. Nat Genet 2015
235
31

Telomerase mutations in smokers with severe emphysema.
Susan E Stanley, Julian J L Chen, Joshua D Podlevsky, Jonathan K Alder, Nadia N Hansel, Rasika A Mathias, Xiaodong Qi, Nicholas M Rafaels, Robert A Wise, Edwin K Silverman,[...]. J Clin Invest 2015
97
29

Short telomeres are a risk factor for idiopathic pulmonary fibrosis.
Jonathan K Alder, Julian J-L Chen, Lisa Lancaster, Sonye Danoff, Shu-chih Su, Joy D Cogan, Irma Vulto, Mingyi Xie, Xiaodong Qi, Rubin M Tuder,[...]. Proc Natl Acad Sci U S A 2008
454
29

Telomere lengths, pulmonary fibrosis and telomerase (TERT) mutations.
Alberto Diaz de Leon, Jennifer T Cronkhite, Anna-Luise A Katzenstein, J David Godwin, Ganesh Raghu, Craig S Glazer, Randall L Rosenblatt, Carlos E Girod, Edward R Garrity, Chao Xing,[...]. PLoS One 2010
206
29


The short and long telomere syndromes: paired paradigms for molecular medicine.
Susan E Stanley, Mary Armanios. Curr Opin Genet Dev 2015
67
27

Telomere phenotypes in females with heterozygous mutations in the dyskeratosis congenita 1 (DKC1) gene.
Jonathan K Alder, Erin M Parry, Srinivasan Yegnasubramanian, Christa L Wagner, Lawrence M Lieblich, Robert Auerbach, Arleen D Auerbach, Sarah J Wheelan, Mary Armanios. Hum Mutat 2013
57
27

X-linked dyskeratosis congenita is caused by mutations in a highly conserved gene with putative nucleolar functions.
N S Heiss, S W Knight, T J Vulliamy, S M Klauck, S Wiemann, P J Mason, A Poustka, I Dokal. Nat Genet 1998
628
27

The telomere syndromes.
Mary Armanios, Elizabeth H Blackburn. Nat Rev Genet 2012
547
25

Adult-onset pulmonary fibrosis caused by mutations in telomerase.
Kalliopi D Tsakiri, Jennifer T Cronkhite, Phillip J Kuan, Chao Xing, Ganesh Raghu, Jonathan C Weissler, Randall L Rosenblatt, Jerry W Shay, Christine Kim Garcia. Proc Natl Acad Sci U S A 2007
552
25

Rare variants in RTEL1 are associated with familial interstitial pneumonia.
Joy D Cogan, Jonathan A Kropski, Min Zhao, Daphne B Mitchell, Lynette Rives, Cheryl Markin, Errine T Garnett, Keri H Montgomery, Wendi R Mason, David F McKean,[...]. Am J Respir Crit Care Med 2015
105
25

Danazol Treatment for Telomere Diseases.
Danielle M Townsley, Bogdan Dumitriu, Delong Liu, Angélique Biancotto, Barbara Weinstein, Christina Chen, Nathan Hardy, Andrew D Mihalek, Shilpa Lingala, Yun Ju Kim,[...]. N Engl J Med 2016
164
25

Diagnostic utility of telomere length testing in a hospital-based setting.
Jonathan K Alder, Vidya Sagar Hanumanthu, Margaret A Strong, Amy E DeZern, Susan E Stanley, Clifford M Takemoto, Ludmila Danilova, Carolyn D Applegate, Stephen G Bolton, David W Mohr,[...]. Proc Natl Acad Sci U S A 2018
71
25

Telomere shortening in familial and sporadic pulmonary fibrosis.
Jennifer T Cronkhite, Chao Xing, Ganesh Raghu, Kelly M Chin, Fernando Torres, Randall L Rosenblatt, Christine Kim Garcia. Am J Respir Crit Care Med 2008
314
23

Telomere-related lung fibrosis is diagnostically heterogeneous but uniformly progressive.
Chad A Newton, Kiran Batra, Jose Torrealba, Julia Kozlitina, Craig S Glazer, Carlos Aravena, Keith Meyer, Ganesh Raghu, Harold R Collard, Christine Kim Garcia. Eur Respir J 2016
125
23

Clinical outcomes of lung transplant recipients with telomerase mutations.
Sofya Tokman, Jonathan P Singer, Megan S Devine, Glen P Westall, John-David Aubert, Michael Tamm, Gregory I Snell, Joyce S Lee, Hilary J Goldberg, Jasleen Kukreja,[...]. J Heart Lung Transplant 2015
46
21




Flow cytometry and FISH to measure the average length of telomeres (flow FISH).
Gabriela M Baerlocher, Irma Vulto, Gary de Jong, Peter M Lansdorp. Nat Protoc 2006
278
17


Haploinsufficiency of telomerase reverse transcriptase leads to anticipation in autosomal dominant dyskeratosis congenita.
Mary Armanios, Jiunn-Liang Chen, Yen-Pei Christy Chang, Robert A Brodsky, Anita Hawkins, Constance A Griffin, James R Eshleman, Alan R Cohen, Aravinda Chakravarti, Ada Hamosh,[...]. Proc Natl Acad Sci U S A 2005
292
17

Heterozygous RTEL1 mutations are associated with familial pulmonary fibrosis.
Caroline Kannengiesser, Raphael Borie, Christelle Ménard, Marion Réocreux, Patrick Nitschké, Steven Gazal, Hervé Mal, Camille Taillé, Jacques Cadranel, Hilario Nunes,[...]. Eur Respir J 2015
85
17

Very short telomere length by flow fluorescence in situ hybridization identifies patients with dyskeratosis congenita.
Blanche P Alter, Gabriela M Baerlocher, Sharon A Savage, Stephen J Chanock, Babette B Weksler, Judith P Willner, June A Peters, Neelam Giri, Peter M Lansdorp. Blood 2007
234
17

Severe hematologic complications after lung transplantation in patients with telomerase complex mutations.
Raphael Borie, Caroline Kannengiesser, Sandrine Hirschi, Jérôme Le Pavec, Hervé Mal, Emmanuel Bergot, Stéphane Jouneau, Jean-Marc Naccache, Patrick Revy, David Boutboul,[...]. J Heart Lung Transplant 2015
61
17

Prevalence and characteristics of TERT and TERC mutations in suspected genetic pulmonary fibrosis.
Raphael Borie, Laure Tabèze, Gabriel Thabut, Hilario Nunes, Vincent Cottin, Sylvain Marchand-Adam, Grégoire Prevot, Abdellatif Tazi, Jacques Cadranel, Herve Mal,[...]. Eur Respir J 2016
58
17

Telomere shortening and tumor formation by mouse cells lacking telomerase RNA.
M A Blasco, H W Lee, M P Hande, E Samper, P M Lansdorp, R A DePinho, C W Greider. Cell 1997
14

Ancestral mutation in telomerase causes defects in repeat addition processivity and manifests as familial pulmonary fibrosis.
Jonathan K Alder, Joy D Cogan, Andrew F Brown, Collin J Anderson, William E Lawson, Peter M Lansdorp, John A Phillips, James E Loyd, Julian J-L Chen, Mary Armanios. PLoS Genet 2011
70
14

Cancer in dyskeratosis congenita.
Blanche P Alter, Neelam Giri, Sharon A Savage, Philip S Rosenberg. Blood 2009
288
14

Telomerase gene mutations are associated with cirrhosis formation.
Daniel Hartmann, Ujala Srivastava, Michaela Thaler, Karin N Kleinhans, Gisèle N'kontchou, Annika Scheffold, Kerstin Bauer, Ramona F Kratzer, Natalia Kloos, Sarah-Fee Katz,[...]. Hepatology 2011
94
14

Disease-specific hematopoietic cell transplantation: nonmyeloablative conditioning regimen for dyskeratosis congenita.
A C Dietz, P J Orchard, K S Baker, R H Giller, S A Savage, B P Alter, J Tolar. Bone Marrow Transplant 2011
94
14

Response to androgen therapy in patients with dyskeratosis congenita.
Payal P Khincha, Ingrid M Wentzensen, Neelam Giri, Blanche P Alter, Sharon A Savage. Br J Haematol 2014
55
14

Liver Transplantation After Bone Marrow Transplantation for End Stage Liver Disease with Severe Hepatopulmonary Syndrome in Dyskeratosis Congenita: A Literature First.
Shyam Sunder Mahansaria, Senthil Kumar, Kishore G S Bharathy, Sachin Kumar, Viniyendra Pamecha. J Clin Exp Hepatol 2015
15
46

Short telomere syndromes cause a primary T cell immunodeficiency.
Christa L Wagner, Vidya Sagar Hanumanthu, C Conover Talbot, Roshini S Abraham, David Hamm, Dustin L Gable, Christopher G Kanakry, Carolyn D Applegate, Janet Siliciano, J Brooks Jackson,[...]. J Clin Invest 2018
38
18

Cancer in the National Cancer Institute inherited bone marrow failure syndrome cohort after fifteen years of follow-up.
Blanche P Alter, Neelam Giri, Sharon A Savage, Philip S Rosenberg. Haematologica 2018
93
14

Radiation Sensitivity and Radiation Necrosis in the Short Telomere Syndromes.
Susan E Stanley, Avani Dholakia Rao, Dustin L Gable, Sharon McGrath-Morrow, Mary Armanios. Int J Radiat Oncol Biol Phys 2015
14
42

Telomere dysfunction causes alveolar stem cell failure.
Jonathan K Alder, Christina E Barkauskas, Nathachit Limjunyawong, Susan E Stanley, Frant Kembou, Rubin M Tuder, Brigid L M Hogan, Wayne Mitzner, Mary Armanios. Proc Natl Acad Sci U S A 2015
161
12

Decreased dyskerin levels as a mechanism of telomere shortening in X-linked dyskeratosis congenita.
Erin M Parry, Jonathan K Alder, Stella S Lee, John A Phillips, James E Loyd, Priya Duggal, Mary Armanios. J Med Genet 2011
38
15

Syndromes of telomere shortening.
Mary Armanios. Annu Rev Genomics Hum Genet 2009
228
12

Outcomes of allogeneic hematopoietic cell transplantation in patients with dyskeratosis congenita.
Shahinaz M Gadalla, Carmem Sales-Bonfim, Jeanette Carreras, Blanche P Alter, Joseph H Antin, Mouhab Ayas, Prasad Bodhi, Jeffrey Davis, Stella M Davies, Eric Deconinck,[...]. Biol Blood Marrow Transplant 2013
66
12

Telomere length is a determinant of emphysema susceptibility.
Jonathan K Alder, Nini Guo, Frant Kembou, Erin M Parry, Collin J Anderson, Amany I Gorgy, Michael F Walsh, Thomas Sussan, Shyam Biswal, Wayne Mitzner,[...]. Am J Respir Crit Care Med 2011
156
12

Clinical and pathologic features of familial interstitial pneumonia.
Mark P Steele, Marcy C Speer, James E Loyd, Kevin K Brown, Aretha Herron, Susan H Slifer, Lauranell H Burch, Momen M Wahidi, John A Phillips, Thomas A Sporn,[...]. Am J Respir Crit Care Med 2005
258
12

A novel dyskerin (DKC1) mutation is associated with familial interstitial pneumonia.
Jonathan A Kropski, Daphne B Mitchell, Cheryl Markin, Vasiliy V Polosukhin, Leena Choi, Joyce E Johnson, William E Lawson, John A Phillips, Joy D Cogan, Timothy S Blackwell,[...]. Chest 2014
75
12


Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.